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棉酚及其衍生物的结构、性质——从生理活性到药物发现和药物设计。

Structure, properties of gossypol and its derivatives-from physiological activities to drug discovery and drug design.

机构信息

School of Materials and Energy, University of Electronic Science and Technology of China, Chengdu 611731, China.

State Key Laboratory of Chemistry and Utilization of Carbon-based Energy Resource, School of Chemistry and Chemical Engineering, Xinjiang University, Urumqi, China.

出版信息

Nat Prod Rep. 2022 Jun 22;39(6):1282-1304. doi: 10.1039/d1np00080b.

Abstract

Covering up to 2022Gossypol is a polyphenolic compound isolated from cottonseed. There are two optical enantiomers of gossypol, (-)-gossypol and (+)-gossypol. Gossypol exists as three different tautomers, aldehyde, ketone and lactol. Gossypol is toxic and provides a protective mechanism for cotton plants against pests. Gossypol was used as a male contraceptive in China in the 1970s. It was eventually abandoned due to noticeable side effects, disruption of potassium uptake and incomplete reversibility. Gossypol has gained considerable research interest due to its attractive biological activities, especially antitumor and antivirus. Gossypol derivatives are prepared by a structural modification to reduce toxicity and improve their therapeutic effect. This review depicts the bioactivity and regulation mechanisms of gossypol and its derivatives as drug lead compounds, with emphasis on its antitumor mechanism. The design and synthesis of pharmacologically active derivatives based on the structure of gossypol, such as gossypol Schiff bases, apogossypol, gossypolone, are thoroughly discussed. This review aims to serve as a reference for gossypol-based drug discovery and drug design.

摘要

棉酚是一种从棉籽中分离得到的多酚类化合物。棉酚有两种光学对映异构体,(-)-棉酚和(+)-棉酚。棉酚存在三种不同的互变异构体,醛、酮和内半缩醛。棉酚具有毒性,为棉花植物提供了一种抵御害虫的保护机制。20 世纪 70 年代,棉酚曾在中国被用作男性避孕药。但由于其明显的副作用、钾吸收的干扰和不完全的可逆性,最终被弃用。由于其具有吸引人的生物活性,特别是抗肿瘤和抗病毒活性,棉酚引起了相当大的研究兴趣。棉酚衍生物通过结构修饰来降低毒性,提高治疗效果。本文综述了棉酚及其衍生物作为药物先导化合物的生物活性和调节机制,重点介绍了其抗肿瘤机制。深入讨论了基于棉酚结构设计和合成的具有药理活性的衍生物,如棉酚席夫碱、去甲棉酚、棉酚酮。本文旨在为基于棉酚的药物发现和药物设计提供参考。

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